홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Sodium Iodide → N-butyl-5-iodo-N-methyl-pentanesulfonamide

HRID 742951
노트
인쇄 미리보기

반응식

HRID 742951 반응식
[I-:1].[Na+].[CH2:3]([N:7]([CH3:17])[S:8]([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15]Cl)(=[O:10])=[O:9])[CH2:4][CH2:5][CH3:6]>C(C(C)=O)C>[CH2:3]([N:7]([CH3:17])[S:8]([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][I:1])(=[O:10])=[O:9])[CH2:4][CH2:5][CH3:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5238Sodium IodideHCID 19711033N-butyl-5-chloro-N-methyl-pentanesulfonamide

생성물 1

HCID 19711034N-butyl-5-iodo-N-methyl-pentanesulfonamide수율 93.8%

시약·촉매·용매 1

HCID 6569Methyl Ethyl Ketone용매

실험 절차

526 mg of sodium iodide were added to a solution of 449 mg of the product of Step A in 4.5 ml of methyl ethyl ketone, and the mixture was stirred at reflux for 4 hours. After cooling, the methyl ethyl ketone was evaporated under reduced pressure and water was added. Extraction was carried out with ethyl acetate and the extracts were washed with water, then with a saturated aqueous solution of sodium chloride, dried and evaporated to dryness under reduced pressure to obtain 572 mg of the expected product.

후처리

  1. temperatureat reflux for 4 hours
  2. temperatureAfter cooling
  3. customthe methyl ethyl ketone was evaporated under reduced pressure and water
  4. additionwas added
  5. extractionExtraction
  6. washthe extracts were washed with water
  7. dry with materialwith a saturated aqueous solution of sodium chloride, dried
  8. customevaporated to dryness under reduced pressure

출처 및 근거

ORD 기록
ord-23d789ad91c24812bc180d0a32b101da
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05556845

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트